Canonical Allele Identifier: PA1139704037
Gene: PEX16 HGNC NCBI

Linked Data

ClinVar Variation Id: 953107
ClinVar RCV Id: RCV001225350
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004804.2:p.Gly336Arg
CA5959716
NM_004813.4:c.1006G>C